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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227036Generated: November 2, 2026

Triethylamine → N-[3-(Bromomethyl)phenyl]-4-(tetradecyloxy)-benzeneacetamide

https://huagongshe.com/reaction/2227036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantLithium BromideHCID 82050—
ReactantHCID 86745364HCID 86745364—
SolventTetrahydrofuranHCID 8028—
ProductN-[3-(Bromomethyl)phenyl]-4-(tetradecyloxy)-benzeneacetamideHCID 10052253—

Reaction Steps

To a stirred solution of 4.0 g of N-[3-hydroxymethyl)phenyl]-4-(tetradecyloxy)-benzeneacetamide in 100 ml of tetrahydrofuran is added 1.19 g of triethylamine followed by 1.34 g of methanesulfonyl chloride. Also added is 7.66 g of lithium bromide and continued stirring for 24 hours. The solvent is removed under vacuum and the residue is partitioned between chloroform and water followed by an additional wash of the organic layer with saturated sodium bicarbonate. The organic layer is dried and filtered through a pad of silica gel. The filtrate is evaporated to a residue which is crystallized from hexane:carbon tetrachloride to give 4.1 g of the desired product as a white powder, m.p. 116°-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350759
Source datasetuspto-grants-1994_09
ORD IDord-b12643036663415aba7eb21d71764258
Source noteuspto-grants-1994_09